What are the responsibilities and job description for the Study Coordinator position at Trinity Employment Specialists?
Job Title: Study Coordinator
Pay: $18/hour
Schedule: Monday–Thursday, 8:00 AM–5:00 PM
Job Type: Full-time, Clinical Research Support
Study Coordinator – Must-Have Requirements
- Must be dependable and punctual for scheduled study visits
- Must be comfortable working in a clinical patient-facing environment
- Must be willing to learn or already capable of taking vital signs
- Must be willing to learn or already capable of performing ECGs
- Must be comfortable with phone communication and patient follow-up
- Must be able to accurately document and enter data
- Must have strong attention to detail
Study Coordinator – Position Summary
We are seeking a Study Coordinator to support clinical research studies in an outpatient clinical setting. This role is ideal for someone with a medical assistant, CNA, or similar clinical background, but training is available for the right candidate.
The Study Coordinator will assist with patient visits, clinical procedures, scheduling, and data entry. This role is essential in ensuring smooth study operations and accurate research data collection.
Study Coordinator – Essential Duties & Responsibilities
- Take and record patient vital signs
- Perform ECGs (training provided if needed)
- Schedule and confirm patient appointments
- Conduct phone triage and patient callbacks
- Check patients in and out for study visits
- Enter clinical and research data accurately
- File and organize study documentation
- Support overall patient flow and study coordination
Study Coordinator – Additional Qualifications
- Medical certification preferred (CMA, CNA, MA, or equivalent)
- Strong communication and interpersonal skills
- Ability to multitask in a clinical environment
- Basic computer and data entry proficiency
- Willingness to learn clinical procedures if not already experienced
- Professional, reliable, and team-oriented attitude
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